EP0550346B1 - Procédé de préparation de matériau composite formé d'un élastomère vulcanisé associe à un élastomère thermoplastique à séquences polyamides; et matériau composite ainsi constitué - Google Patents

Procédé de préparation de matériau composite formé d'un élastomère vulcanisé associe à un élastomère thermoplastique à séquences polyamides; et matériau composite ainsi constitué Download PDF

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Publication number
EP0550346B1
EP0550346B1 EP92403586A EP92403586A EP0550346B1 EP 0550346 B1 EP0550346 B1 EP 0550346B1 EP 92403586 A EP92403586 A EP 92403586A EP 92403586 A EP92403586 A EP 92403586A EP 0550346 B1 EP0550346 B1 EP 0550346B1
Authority
EP
European Patent Office
Prior art keywords
elastomer
composite material
thermoplastic elastomer
elastomers
polyamide blocks
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP92403586A
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German (de)
English (en)
French (fr)
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EP0550346A1 (fr
Inventor
Marius Hert
Patrick Alex
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Arkema France SA
Original Assignee
Atofina SA
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Filing date
Publication date
Application filed by Atofina SA filed Critical Atofina SA
Publication of EP0550346A1 publication Critical patent/EP0550346A1/fr
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Publication of EP0550346B1 publication Critical patent/EP0550346B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B25/00—Layered products comprising a layer of natural or synthetic rubber
    • B32B25/04—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B25/08—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
    • B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B25/00—Layered products comprising a layer of natural or synthetic rubber
    • B32B25/14—Layered products comprising a layer of natural or synthetic rubber comprising synthetic rubber copolymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/12—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0016—Plasticisers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L13/00—Compositions of rubbers containing carboxyl groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/02—Copolymers with acrylonitrile
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B38/00—Ancillary operations in connection with laminating processes
    • B32B2038/0052—Other operations not otherwise provided for
    • B32B2038/0076—Curing, vulcanising, cross-linking
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2305/00—Condition, form or state of the layers or laminate
    • B32B2305/72—Cured, e.g. vulcanised, cross-linked
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2437/00—Clothing
    • B32B2437/02—Gloves, shoes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2321/00—Characterised by the use of unspecified rubbers

Definitions

  • the present invention relates to a method of preparation of composite material formed of an elastomer vulcanized, containing carboxylic acid functions or dicarboxylic acid anhydride, associated with a thermoplastic elastomer with polyamide blocks. She also relates to the composite material consisting of a vulcanized elastomer combined with an elastomer thermoplastic with polyamide blocks and articles of sports, in particular the soles of sports shoes, made at least in part of such a material.
  • European patent application No. 0 344 427 describes a process for vulcanizing a rigid thermoplastic containing at least 30% of aliphatic polyamide with a rubber-based composition, only in the presence of peroxides as a vulcanizing agent. This process makes it possible to obtain composite materials with cohesive failure, resistant to solvents and atmospheric conditions, usable for making cables, tubes, conveyor belts or seals. We also know the reactivity of certain elastomers on polymers based on polyetheresteramide.
  • Japanese patent JP 63 081159 (Derwent 88-038019 / 20) describes a thermoplastic elastomer composition comprising a polyetheresteramide component and an elastomer having at least one polar group such as a carboxylic radical.
  • thermoplastic elastomers have flexibility high, good oil resistance and resistance high mechanical.
  • One of the objects of the present invention is to propose a process for preparing composite material as defined above, avoiding the application of a adhesive.
  • Another object of the present invention is to propose a process for preparing composite material as mentioned above, which can be industrialized, i.e. with a short cycle time (usually not exceeding 15 minutes).
  • Another object of the present invention is to propose a composite material as defined above, especially intended for the production of soles sports shoes with cohesive rupture in the vulcanized elastomer during the stress on the separation.
  • the method of preparation is that a composition elastomer comprising a synthetic elastomer or natural containing carboxylic acid functions or dicarboxylic acid anhydride, a system of crosslinking and possibly various adjuvants and fillers are vulcanized in a mold, part of which is occupied by a sequence thermoplastic elastomer polyamides, the vulcanization temperature being between - 15 ° C and + 5 ° C from the Vicat point of said thermoplastic elastomer having polyamide blocks.
  • the elastomeric composition and kinetics of vulcanization are such that the material has a cohesive rupture in the vulcanized elastomer during a stress on the separation of the two elastomers.
  • the vulcanized and thermoplastic elastomers forming the composite material are normally sufficiently strongly associated to prevent separation during normal effort, taking into account desired use.
  • separation implies the application of considerably more force to the material higher than that to which said material should normally be subjected.
  • Synthetic or natural vulcanizable elastomers suitable for the implementation of the present invention are well known from those skilled in the art, the term elastomer in the definition of this invention meaning that it can consist of mixtures of several elastomers.
  • elastomers or mixtures of elastomers have a remanent compression deformation (D.R.C.) at 100 ° C less than 50% generally between 5 and 40% and preferably less than 30%.
  • D.R.C. remanent compression deformation
  • elastomers carboxylated nitriles, acrylic elastomers, polybutadienes carboxylated, grafted ethylene / propylene / diene terpolymers or mixtures of these polymers with the same elastomers but not grafted such as nitrile rubbers, polybutadienes, terpolymers ethylene / propylene / diene, alone or as a mixture.
  • the aforementioned vulcanizable elastomers comprise a weight ratio of carboxylic acid or diacid anhydride radicals carboxylic between 0.3 and 10% relative to said elastomers.
  • Vulcanization systems suitable for this invention are well known to those skilled in the art and therefore the invention is not limited to a particular type of system. It is sufficient that this meets the criterion concerning the defined vulcanization kinetics in the definition of the invention indicated above.
  • the elastomer is acrylic (polybutylacrylate with acid or epoxy functions or any other reactive function allowing the crosslinking) we use the usual crosslinking agents based on diamines (orthotoluidyl guanidine, diphenylguanidine, etc.) or blocked diamines (hexamethylene diamine carbamate, etc.).
  • the elastomeric compositions can be modified for certain specific properties (improvement of mechanical properties for example) by the addition of fillers such as carbon black, silica, kaolin, aluminum, clay, talc, chalk, etc. These charges can be treated on the surface by silanes, polyethylene glycols or any other coupling molecule. In general, the rate of charges in parts by weight is between 5 and 100 percent parts of elastomers.
  • compositions can be softened by plasticizers such as mineral oils petroleum derivatives, phthalic acid esters or sebacic acid, liquid polymer plasticizers such as possibly low mass polybutadiene carboxylated, and other well known plasticizers from the skilled person.
  • plasticizers such as mineral oils petroleum derivatives, phthalic acid esters or sebacic acid, liquid polymer plasticizers such as possibly low mass polybutadiene carboxylated, and other well known plasticizers from the skilled person.
  • the vulcanizing agent combinations used to implement the process are such that they must allow complete crosslinking of the elastomer according to kinetics leading to good properties of resistance to separation, such as mentioned in the definition of the invention and in general, with good rubber properties (measured by a residual compression deformation at 100 ° C, dynamometric properties in traction, etc.).
  • the vulcanization temperature is between - 15 ° C and + 0 ° C relative to the Vicat point of thermoplastic elastomer with polyamide blocks.
  • the vulcanization temperature in the mold will be advantageously between 130 and 180 ° C.
  • the kinetics measured using an oscillating rheometer will be such that the characteristic vulcanization time at 90%, t 90 , does not exceed 15 minutes and advantageously will be between 5 and 10 minutes.
  • the time to vulcanization start (or setting time) corresponding to an increase in torque of 0.2 N.m was an important factor in obtaining materials with good performance. So it is advantageous that the increase of the above torque is reached in a time greater than or equal to 4 minutes at molding temperature and preferably between 4 and 6 minutes.
  • the Vicat point is the temperature at which a needle having a circular cross section of 1 mm 2 penetrates 1 mm deep in the sample during a temperature rise of 50 ° C per hour according to the ASTM D1525 standard. Thus, at this temperature, the polymer does not creep and is not in the molten state.
  • Polyamide block thermoplastic elastomers are those whose polyamide sequences are separated by sequences different such as polyester, polyether, polyurethane for example.
  • Thermoplastic elastomers with polyamide blocks advantageously used to implement the method are polyethers containing polyamide blocks (or polyetheramides).
  • polyethers containing polyamide blocks means both polyethers with statistical polyamide blocks (that is to say formed by the sequence of the various monomer constituents) that the polyethers to block polyamide blocks, that is to say blocks having a certain chain length of their various constituents.
  • the polyetheramide is a block polyetheresteramide of molecular weight greater than 10,000, formed from the product of the co-polycondensation of a polyamide or alpha-omega dicarboxylic copolyamide with molecular weight from 300 to 15,000 and, preferably, 600 to 5,000, employed at a rate of 95 to 15 % by weight and of a polyetherdiol having a molecular weight of 100 to 6000 and, preferably 200 to 3000, used at a rate of 5 to 85% by weight.
  • polyethers mention may be made of polyoxyethylene glycol, polyoxypropylene glycol, polyoxytetramethylene glycol, having a weight average molecular between 100 and 6000, preferably between 200 and 3000. These polyethers can also result from mixtures of polymers cited above. The lengthening of the polyether chains is ensured by ester bonds.
  • these polyethers containing polyamide blocks will have a Vicat point between 100 and 200 ° C, preferably between 130 and 175 ° C and a melting point between 120 and 210 ° C and preferably between 140 and 180 ° C.
  • the process consists of forming an elastomer thermoplastic with polyamide blocks and in particular a block polyether polyamides then to dispose by a suitable means the thermoplastic elastomer with polyamide sequences in a vulcanization mold, preferably, so that it is affixed against one of the walls of the mold.
  • a suitable means the thermoplastic elastomer with polyamide sequences in a vulcanization mold, preferably, so that it is affixed against one of the walls of the mold.
  • the elastomer is a film
  • Its thickness will preferably vary between 0.3 and 5 mm, advantageously less than or equal to 1 mm.
  • the width of the film is variable, and it can be punched out.
  • the film piece is then positioned against at least part of the wall of the mold vulcanization of the elastomer, in a known manner.
  • the film pieces can also be stored for the desired time.
  • thermoplastic elastomer is formed of a element of defined shape, for example in the form of a cut profile, this is preferably affixed to the bottom of the mold.
  • the mold is fitted with impression covers of the elastomer part which are removed after injection of the thermoplastic to allow the injection of the elastomer.
  • the elastomeric composition comprising the elastomer with its fillers, plasticizers and other additives, but without the crosslinking is formulated in a suitable reactor, then it is taken up possibly in another mixer, at an appropriate temperature with the vulcanization system.
  • the molding of the elastomer and its vulcanization is made in the mold, part of which is occupied by the workpiece polyether with polyamide blocks, as indicated above, according to one of classic rubber industry processes: simple compression, compression transfer, injection, transfer injection. In general, it takes place in a steel compression mold, with a thickness of a few millimeters, placed between two heating plates of a press. The amount of elastomeric composition introduced into the mold can slightly exceed the volume of the imprint. Closing the press causes the elastomer to creep into the mold and evacuate the excess elastomer through the overflow channels. Thus, after distribution of material, and taking into account the geometry of the mold, the pressure on the elastomeric composition is low (close to atmospheric pressure).
  • the materials obtained exhibited excellent properties in the case where the temperature of the tray, top of the mold, was equal to the Vicat temperature of thermoplastic elastomer at more or less 5 ° C, and the temperature of the bottom pan of the mold was between the Vicat temperature of the thermoplastic elastomer and the Vicat temperature reduced by 15 ° C.
  • the part is removed.
  • thermoplastic elastomer is a film
  • E being the thickness in mm.
  • the invention also relates to a material composite formed of a vulcanized elastomer containing carboxylic acid or diacid anhydride functions carboxylic, directly associated with an elastomer thermoplastic with polyamide blocks having a point of melting between 120 and 210 ° C and a Vicat point between 100 ° C and 200 ° C, said composite material with a cohesive rupture inside the vulcanized elastomer during a stress on the separation.
  • Vulcanized elastomers are those which have previously described during the presentation of the process for preparing the composite material, including the variants concerning the addition of charges or plasticizers in particular.
  • the polyamide sequence will be chosen among polyamides 6, 11 or 12 and the sequences polyethers will be chosen from polyethylenes oxides, polypropylenes oxides and polytetramethylene oxides or a mixture of these different molecular weight units between 100 and 6,000.
  • the resistance to separation will be measured by the peel test.
  • the peel strength will advantageously be greater than 6 daN / cm.
  • thermoplastic elastomer with polyamide blocks is a block or object having a defined shape, for example, a submerged reinforcing element partially or inserted into the vulcanized elastomer, the tensile strength. This will vary depending on the form of the article.
  • the invention finds a particularly interesting application for the production of sporting goods, at least part of which is made of a composite material as defined above.
  • the invention is thus advantageously adapted to the realization of soles of sports shoes at least part of which is made of elastomer vulcanized comprising one or more elastomer reinforcement elements thermoplastic as described above.
  • the elastomeric composition without the crosslinking is formulated on an internal Repiquet K1 mixer of 3.5 liters, whose rotors rotate at 60 rpm.
  • the operation is done in regime semi-adiabatic, with transformation of mechanical energy into heat.
  • An intimate mixture is obtained in less than 5 minutes and the temperature reaches 110 ° C.
  • the elastomer thus formulated is then taken up on a mixer with cyclinders heated to 80 ° C and the vulcanization system is added to it.
  • thermoplastic elastomer part with polyamide sequences by the elastomeric composition is carried out in a steel compression mold, placed between the two heating plates of a press.
  • the peel strength is measured after 24 hours. Fur is started by leaving an area without adhesion between elastomers vulcanized and polyether to polyamide blocks with adhesive tape of aluminum placed on the polyether with polyamide blocks before molding of the elastomer.
  • Example 1 is reproduced with the difference ready that we use elastomer butadiene-acrylonitrile-acrylic acid terpolymer 69/24/7 as the sole elastomer.
  • This elastomer has a setting time of 4 minutes 20 seconds 3 160 ° C.
  • Example 1 is reproduced apart from the fact that the terpolymer butadiene-acrylonitrile-acrylic acid 69/24/7 is replaced by a 73/27 acrylonitrile butadiene copolymer in the same proportions.
  • Example 4 is reproduced apart from the fact that the butadiene-acrylonitrile-acrylic acid 69/24/7 terpolymer is replaced by the butadiene-styrene copolymer 85/15 in the same quantities which leads to 100 parts of the latter copolymer .
  • Examples 7, 8, 9 below are intended to illustrate the influence the processing temperature as a function of the Vicat point of the polyether with polyamide blocks (PEBA).
  • Example 2 has been reproduced apart from the fact that the temperature of the bottom plate is 150 ° C (instead of 155 ° C in Example 1).
  • the peel strength in daN / cm is 8.5 and the break is cohesive.
  • Example 2 has been reproduced apart from the fact that the PEBA used is marketed under the brand name PEBAX 5533 and has a Vicat point of 144 ° C and that the temperatures of the high and low plates were modified, 140 and 140 respectively.
  • the peeling force in daN / cm is 10.75 and the rupture is cohesive.
  • Example 2 has been reproduced apart from the fact that the PEBA used is marketed under the brand name PEBAX 7033 and has a Vicat point of 165 ° C and that the temperatures of the high and low plates were modified, at 165 and 155 respectively.
  • the peeling force in daN / cm is 8 and the rupture is cohesive.
  • a semicircular part 2 mm thick is made by thermoplastic injection molding, with PEBAX 6333.
  • the piece in PEBAX is inserted in the imprint of the low tray an elastomer mold whose top plate is equipped with four footprints in the form of 6 mm high studs identical to the studs on soles of football boots. These footprints are fed by through nozzles connected to the transfer pot by a system of cylindrical channels.
  • the injection takes place at a material temperature of 120 ° C and a piston speed of 30 mm / s.
  • High and low shelf temperatures are respectively 160 ° and 155 ° C and the part is removed from the mold after 6 minutes.
  • the part thus obtained has a cohesive rupture in the rubber when making a dynamometric test of tearing of the stud.
  • the composite part has good abrasion resistance and the elasticity in compression of nitrile rubber while PEBAX brings dynamic mechanical properties, lightness and comfort foot.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Thermal Sciences (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Laminated Bodies (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
  • Injection Moulding Of Plastics Or The Like (AREA)
  • Reinforced Plastic Materials (AREA)
EP92403586A 1991-12-31 1992-12-30 Procédé de préparation de matériau composite formé d'un élastomère vulcanisé associe à un élastomère thermoplastique à séquences polyamides; et matériau composite ainsi constitué Expired - Lifetime EP0550346B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9116400 1991-12-31
FR9116400A FR2685660A1 (fr) 1991-12-31 1991-12-31 Procede de preparation de materiau composite forme d'un elastomere vulcanise associe a un elastomere thermoplastique a sequences polyamides et materiau composite ainsi constitue.

Publications (2)

Publication Number Publication Date
EP0550346A1 EP0550346A1 (fr) 1993-07-07
EP0550346B1 true EP0550346B1 (fr) 2001-07-18

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EP92403586A Expired - Lifetime EP0550346B1 (fr) 1991-12-31 1992-12-30 Procédé de préparation de matériau composite formé d'un élastomère vulcanisé associe à un élastomère thermoplastique à séquences polyamides; et matériau composite ainsi constitué

Country Status (9)

Country Link
US (1) US5624994A (enrdf_load_stackoverflow)
EP (1) EP0550346B1 (enrdf_load_stackoverflow)
JP (1) JP2957829B2 (enrdf_load_stackoverflow)
KR (1) KR0165130B1 (enrdf_load_stackoverflow)
AT (1) ATE203198T1 (enrdf_load_stackoverflow)
CA (1) CA2086502C (enrdf_load_stackoverflow)
DE (1) DE69231944T2 (enrdf_load_stackoverflow)
ES (1) ES2158845T3 (enrdf_load_stackoverflow)
FR (1) FR2685660A1 (enrdf_load_stackoverflow)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2700292B1 (fr) * 1993-01-13 1995-02-24 Atochem Elf Sa Article tubulaire composite formé d'un élastomère vulcanisé associé à un élastomère thermoplastique à séquences polyamide, notamment tuyau à essence et procédé de préparation d'un tel article.
CA2166215A1 (fr) * 1993-06-28 1995-01-05 Martine Cerf Structure composite comprenant un elastomere et un polymere thermoplastique, procede de preparation et objet contenant celle-ci
DE69427069T2 (de) 1993-11-26 2001-09-13 Atofina, Puteaux An Thermoplasten haftende Thermoplast-Kautschukpolymerlegierungen
FR2719520A1 (fr) 1994-05-06 1995-11-10 Atochem Elf Sa Matériau comprenant un élastomère vulcanisé associé à un élastomère thermoplastique.
EP0739931A1 (fr) * 1995-04-25 1996-10-30 Elf Atochem S.A. Procédé de surmoulage d'un thermoplastique sur un caoutchouc
NL1004246C2 (nl) * 1996-10-10 1998-04-14 Dsm Nv Gevulcaniseerd rubberprodukt.
WO1998001500A1 (en) * 1996-07-05 1998-01-15 Dsm N.V. Vulcanized rubber product
BR9902743C1 (pt) * 1999-07-13 2001-05-22 Nitriflex S A Ind E Com Composição de copolìmeros de nbr carboxilados ou não e copolìmero de etileno vinil acetato (eva) e composição vulcanizável de copolìmeros de nbr carboxilados ou não e eva
CA2308876A1 (en) * 2000-05-12 2001-11-12 Bayer Inc. Improved rubber composition
US6726985B2 (en) 2000-11-03 2004-04-27 Nathan Amitai Shoe sole
DE10227733A1 (de) * 2002-06-21 2004-01-08 Bayer Ag Copolymere enthaltende Kautschukmischungen für die Herstellung von Reifen
FR2890969A1 (fr) * 2005-09-16 2007-03-23 Arkema Sa Copolymeres a blocs polyamides et blocs polyethers resistants au vieillissement
DE102015111716B4 (de) * 2015-07-20 2021-09-02 Hochschule Kaiserslautern Schuh und Verfahren zu dessen Herstellung

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0344427A2 (de) * 1988-05-28 1989-12-06 Hüls Aktiengesellschaft Verfahren zur Herstellung eines chemischen Verbundes zwischen Formmassen auf Basis von aliphatischen Polyamiden einerseits und Carboxylgruppen enthaltenden Kautschuken andererseits sowie die nach diesem Verfahren hergestellten Werkstoffe

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Publication number Priority date Publication date Assignee Title
GB1387583A (en) * 1971-05-21 1975-03-19 Dunlop Ltd Composite structures
GB1434719A (en) * 1972-09-01 1976-05-05 Raychem Ltd Heat recoverable products
US3972973A (en) * 1973-08-29 1976-08-03 Dunlop Limited Method of making rubber and polyester structures
CA1331737C (en) * 1986-10-30 1994-08-30 Kunihide Hiraoka Laminated and molded article prepared therefrom
US4996263A (en) * 1988-10-06 1991-02-26 The Goodyear Tire & Rubber Company High modulus rubber composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0344427A2 (de) * 1988-05-28 1989-12-06 Hüls Aktiengesellschaft Verfahren zur Herstellung eines chemischen Verbundes zwischen Formmassen auf Basis von aliphatischen Polyamiden einerseits und Carboxylgruppen enthaltenden Kautschuken andererseits sowie die nach diesem Verfahren hergestellten Werkstoffe

Also Published As

Publication number Publication date
CA2086502C (fr) 2000-06-27
FR2685660B1 (enrdf_load_stackoverflow) 1995-04-14
JP2957829B2 (ja) 1999-10-06
FR2685660A1 (fr) 1993-07-02
DE69231944T2 (de) 2002-04-04
US5624994A (en) 1997-04-29
DE69231944D1 (de) 2001-08-23
CA2086502A1 (fr) 1993-07-01
KR930013002A (ko) 1993-07-21
KR0165130B1 (ko) 1999-03-20
EP0550346A1 (fr) 1993-07-07
ATE203198T1 (de) 2001-08-15
JPH06212022A (ja) 1994-08-02
ES2158845T3 (es) 2001-09-16

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